Hashizume T, Shida R, Suzuki S, Kasuya E, Kuwayama H, Suzuki H, Oláh M, Nagy G M
Faculty of Agriculture, Iwate University, Morioka 020-8550, Japan.
Domest Anim Endocrinol. 2008 Apr;34(3):327-32. doi: 10.1016/j.domaniend.2007.09.002. Epub 2007 Oct 15.
We have recently demonstrated that salsolinol (SAL), a dopamine (DA)-derived compound, is present in the posterior pituitary gland and is able to stimulate the release of prolactin (PRL) in ruminants. The aim of the present study was to clarify the effect that the interaction of SAL with thyrotropin-releasing hormone (TRH) or DA has on the secretion of PRL in ruminants. A single intravenous (i.v.) injection of SAL (5mg/kg body weight (b.w.)), TRH (1microg/kg b.w.), and SAL plus TRH significantly stimulated the release of PRL in goats (P<0.05). The cumulative response curve (area under the curve: AUC) during 120min was 1.53 and 1.47 times greater after the injection of SAL plus TRH than either SAL or TRH alone, respectively (P<0.05). A single i.v. injection of sulpiride (a DA receptor antagonist, 0.1mg/kg b.w.), sulpiride plus SAL (5mg/kg b.w.), and sulpiride plus TRH (1microg/kg b.w.) significantly stimulated the release of PRL in goats (P<0.05). The AUC of PRL during 120min was 2.12 and 1.78 times greater after the injection of sulpiride plus TRH than either sulpiride alone or sulpiride plus SAL, respectively (P<0.05). In cultured bovine anterior pituitary (AP) cells, SAL (10(-6)M), TRH (10(-8)M), and SAL plus TRH significantly increased the release of PRL (P<0.05), but the additive effect of SAL and TRH detected in vivo was not observed in vitro. In contrast, DA (10(-6)M) inhibited the TRH-, as well as SAL-induced PRL release in vitro. All together, these results clearly show that SAL can stimulate the release of PRL in ruminants. Furthermore, they also demonstrate that the additive effect of SAL and TRH on the release of PRL detected in vivo may not be mediated at the level of the AP, but that DA can overcome their releasing activity both in vivo and in vitro, confirming the dominant role of DA in the inhibitory regulation of PRL secretion in ruminants.
我们最近证实,从多巴胺(DA)衍生而来的化合物沙芦啉醇(SAL)存在于垂体后叶,并能够刺激反刍动物催乳素(PRL)的释放。本研究的目的是阐明SAL与促甲状腺激素释放激素(TRH)或DA的相互作用对反刍动物PRL分泌的影响。单次静脉注射SAL(5mg/kg体重(b.w.))、TRH(1μg/kg b.w.)以及SAL加TRH,均能显著刺激山羊PRL的释放(P<0.05)。注射SAL加TRH后120分钟内的累积反应曲线(曲线下面积:AUC)分别比单独注射SAL或TRH时大1.53倍和1.47倍(P<0.05)。单次静脉注射舒必利(一种DA受体拮抗剂,0.1mg/kg b.w.)、舒必利加SAL(5mg/kg b.w.)以及舒必利加TRH(1μg/kg b.w.),均能显著刺激山羊PRL的释放(P<0.05)。注射舒必利加TRH后120分钟内PRL的AUC分别比单独注射舒必利或舒必利加SAL时大2.12倍和1.78倍(P<0.05)。在培养的牛垂体前叶(AP)细胞中,SAL(10⁻⁶M)、TRH(10⁻⁸M)以及SAL加TRH均能显著增加PRL的释放(P<0.05),但在体外未观察到在体内检测到的SAL和TRH的相加作用。相反,DA(10⁻⁶M)在体外抑制TRH以及SAL诱导的PRL释放。总之,这些结果清楚地表明SAL能够刺激反刍动物PRL的释放。此外,它们还表明,在体内检测到的SAL和TRH对PRL释放的相加作用可能不是在AP水平介导,但DA在体内和体外均能克服它们的释放活性,证实了DA在反刍动物PRL分泌的抑制调节中的主导作用。